Veronica Loitegui

Veronica Loitegui

Associate Director, Sr. Global Feasibility Lead @ Bristol Myers Squibb

About Veronica Loitegui

Veronica Loitegui is the Associate Director, Sr. Global Feasibility Lead at Bristol Myers Squibb in Princeton, New Jersey, with over 9 years of experience at the company in various roles.

Title

Veronica Loitegui currently holds the position of Associate Director, Sr. Global Feasibility Lead at Bristol Myers Squibb. Based in Princeton, New Jersey, she oversees global feasibility studies and leads initiatives aimed at improving the efficiencies of clinical trials.

Current Company

Veronica Loitegui is employed by Bristol Myers Squibb, a multinational pharmaceutical company known for its innovative work in drug development and healthcare solutions. She has been with the company for over nine years, contributing to various roles within clinical trial analytics, feasibility, and monitoring.

Previous Roles at Bristol Myers Squibb

Veronica Loitegui has held multiple roles at Bristol Myers Squibb over the past nine years. She served as a Feasibility Specialist, Clinical Trial Analytics from 2018 to 2020 in Princeton, New Jersey, focusing on improving trial efficiency. Prior to that, she was a Clinical Site Monitor from 2014 to 2018 in Vicente Lopez, Buenos Aires, responsible for site oversight and operational aspects of clinical trials.

Education and Expertise

Veronica Loitegui earned her Licenciatura en Nutricion from Universidad de Buenos Aires, where she studied from 1996 to 2000. This educational background laid the foundation for her career in clinical research and data management, providing her with a strong understanding of the healthcare and pharmaceutical industries.

Career Background

Veronica started her career at Schering-Plough Research Institute as a Clinical Data Coordinator and later became the Lead Clinical Data Coordinator. She then transitioned to Merck, Sharpe & Dohme (MSD) as a Data Management Specialist (DMS) Lead from 2011 to 2013. Additionally, she served as a Clinical Research Associate II at Novartis for eight months in 2013 before joining Bristol Myers Squibb. Her extensive background in clinical data and site management has been instrumental in her current role.

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